The same FLT3-internal tandem duplication (ITD) positive clone was detected at diagnosis and relapse, but not at birth, in a child with M1 acute myeloid leukemia. Single nucleotide polymorphism arrays demonstrated that chromosome 13 acquired uniparental disomy, in association with del(9q), represented a progressive event in the course of the disease, and it was responsible for the homozygous FLT3-ITD at relapse.

Bungaro, S., Raghavan, M., Dell'Oro, M., Paolucci, P., Young, B., Biondi, A., et al. (2006). Assessment of submicroscopic genetic lesions by single nucleotide polymorphism arrays in a child with acute myeloid leukemia and FLT3-internal tandem duplication. HAEMATOLOGICA, 91(7), 998-1000.

Assessment of submicroscopic genetic lesions by single nucleotide polymorphism arrays in a child with acute myeloid leukemia and FLT3-internal tandem duplication

BIONDI, ANDREA;Cazzaniga, G.
2006

Abstract

The same FLT3-internal tandem duplication (ITD) positive clone was detected at diagnosis and relapse, but not at birth, in a child with M1 acute myeloid leukemia. Single nucleotide polymorphism arrays demonstrated that chromosome 13 acquired uniparental disomy, in association with del(9q), represented a progressive event in the course of the disease, and it was responsible for the homozygous FLT3-ITD at relapse.
Articolo in rivista - Articolo scientifico
Follow-Up Studies; Disease Progression; Oligonucleotide Array Sequence Analysis; Female; Polymorphism, Single Nucleotide; Child; fms-Like Tyrosine Kinase 3; Gene Deletion; Leukemia, Myeloid, Acute; Tandem Repeat Sequences; Humans
English
lug-2006
91
7
998
1000
none
Bungaro, S., Raghavan, M., Dell'Oro, M., Paolucci, P., Young, B., Biondi, A., et al. (2006). Assessment of submicroscopic genetic lesions by single nucleotide polymorphism arrays in a child with acute myeloid leukemia and FLT3-internal tandem duplication. HAEMATOLOGICA, 91(7), 998-1000.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/14909
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